Alkadienes: what they are, examples and isoprene

Alkadienes or dienes are open carbon chain hydrocarbons that have two double bonds.

Generally speaking, the formula for alkadienes is ÇnoH2n-2.

Classification

Alkadienes are classified according to the position of their unsaturation:

  • Accumulated dienes: The two double bonds occur on neighboring carbons.
  • isolated dienes: The two double bonds belong to different carbons, in addition to being separated by at least two single bonds or a saturated carbon.
  • Conjugated dienes: Double bonds appear alternately.

Examples:

1. straight H with 2 subscript straight C equal to straight C equal to CH minus CH with 3 subscript Propadiene or but-1,2-diene (Accumulated Diene)

2. straight H with 2 subscript straight C equal to CH minus CH with 2 subscript minus CH equal to CH with 2 subscript Pent-1,4-diene (isolated diene)

3. straight H with 2 subscript straight C equal to CH minus CH equal to CH with 2 subscript But-1,3-diene (Conjugated Diene)

How is the nomenclature given to alkadienes?

The nomenclature of alkadienes is similar to that of alkenes.

The prefixes are the same as those used in hydrocarbon nomenclature. In this case, we have the following order:

Prefix + dien + o

The term dien represents the presence of double double bonds.

The main chain is the longest and has the two double bonds. Each of the links must be numbered.

Carbon numbering starts from the end closest to the unsaturation.

Furthermore, the numbering must be carried out so that the position of double bonds and branches is as small as possible.

Examples:

1. straight H with 2 subscript straight C equal to straight C equal to CH with 2 subscript propadiene

2. straight H with 2 subscript straight C equal to CH minus CH equal to CH minus CH with 3 subscript pent-1,3-diene

When alkadienes have ramifications, they should also be indicated.

Examples:

1. table row with blank blank blank blank blank blank blank blank row with blank blank cell with CH with 3 subscript end of cell blank blank blank blank blank blank blank line with blank blank vertical line blank blank blank blank blank blank line with cell with straight H with 3 subscript straight C end of cell minus straight C minus cell with CH with 2 subscript end of cell minus CH equal to straight C cell with equal to CH with 2 subscript end of cell row with blank blank vertical row blank blank blank blank blank blank row with blank blank cell with CH with 3 subscript end of cell blank blank blank blank blank blank blank line with blank blank blank blank blank blank blank blank blank line with blank blank blank blank blank blank blank blank blank end of table 5,5-dimethyl-1,2-hexadiene

2. table row with blank blank blank blank blank blank blank blank row with blank blank cell with CH with 3 subscript end of cell blank blank blank blank blank blank row with blank blank vertical row blank blank blank blank blank row with cell with straight H with 2 straight subscript C end of cell equal to straight C minus CH equals cell with CH with 2 subscribed end of cell blank blank line with blank blank blank blank blank blank blank blank line with blank blank blank blank blank blank blank blank blank line with blank blank blank blank blank blank blank line with blank blank blank blank blank blank blank blank line with blank blank blank blank blank blank blank blank end of table2-methyl-but-1,3-diene

Learn more, read also:

  • Hydrocarbons
  • Aromatic hydrocarbons
  • carbon chains
  • Organic chemistry

Isoprene

Isopropene (C5H8) is the most representative alkadiene, characterized as a colorless and volatile organic substance. It is represented as follows:

table row with cell with CH with 2 subscript end of cell equal to straight C minus CH equal to cell with CH with 2 subscript end of cell blank blank blank row with blank blank row vertical blank blank blank blank blank blank line with blank blank cell with CH with 3 subscript end of cell blank blank blank blank blank blank line with blank blank blank blank blank blank blank blank blank blank blank blank blank blank blank blank blank blank blank blank blank blank blank blank blank blank blank blank blank blank blank blank blank blank blank blank blank end of table

The carbon chain representing isoprene results in the following nomenclature: 2-methylbut-1,3-diene.

From various combinations between them, terpenes are formed, a set of substances, which stand out: natural rubber, essential oils, carotenoids and steroids.

The synthetic rubber used in the manufacture of many products is the result of the polymerization of isoprene.

Read too:

  • Carbon
  • alkanes
  • alkenes
  • Alkynes
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